Detalhe da pesquisa
1.
Skin in the game: a review of single-cell and spatial transcriptomics in dermatological research.
Clin Chem Lab Med
; 2024 Apr 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-38656304
2.
MicroRNA-139 Expression Is Dispensable for the Generation of Influenza-Specific CD8+ T Cell Responses.
J Immunol
; 208(3): 603-617, 2022 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35022277
3.
Genetic heterogeneity of heritable ectopic mineralization disorders in a large international cohort.
Genet Med
; 24(1): 75-86, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34906475
4.
Selective inhibition of Ph-positive ALL cell growth through kinase-dependent and -independent effects by CDK6-specific PROTACs.
Blood
; 135(18): 1560-1573, 2020 04 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-32040545
5.
Novel PTCH1 and concurrent TP53 mutations in four patients with numerous non-syndromic basal cell carcinomas: The paradigm of oncogenic synergy.
Exp Dermatol
; 31(5): 736-742, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-34862824
6.
RNA-Binding Protein HuR Promotes Th17 Cell Differentiation and Can Be Targeted to Reduce Autoimmune Neuroinflammation.
J Immunol
; 204(8): 2076-2087, 2020 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-32169842
7.
Whole-Transcriptome Analysis by RNA Sequencing for Genetic Diagnosis of Mendelian Skin Disorders in the Context of Consanguinity.
Clin Chem
; 67(6): 876-888, 2021 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33969388
8.
iSeqQC: a tool for expression-based quality control in RNA sequencing.
BMC Bioinformatics
; 21(1): 56, 2020 Feb 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-32054449
9.
A novel autosomal recessive GJB2-associated disorder: Ichthyosis follicularis, bilateral severe sensorineural hearing loss, and punctate palmoplantar keratoderma.
Hum Mutat
; 40(2): 217-229, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30431684
10.
Autosomal recessive congenital ichthyosis: Genomic landscape and phenotypic spectrum in a cohort of 125 consanguineous families.
Hum Mutat
; 40(3): 288-298, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30578701
11.
Inherited Interleukin 2-Inducible T-Cell (ITK) Kinase Deficiency in Siblings With Epidermodysplasia Verruciformis and Hodgkin Lymphoma.
Clin Infect Dis
; 68(11): 1938-1941, 2019 05 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-30778533
12.
Single-Cell Genomics.
Clin Chem
; 65(8): 972-985, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30872376
13.
Whole exome sequencing identifies a germline MET mutation in two siblings with hereditary wild-type RET medullary thyroid cancer.
Hum Mutat
; 39(3): 371-377, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29219214
14.
Effects of genetic variation in protease activated receptor 4 after an acute coronary syndrome: Analysis from the TRACER trial.
Blood Cells Mol Dis
; 72: 37-43, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30055940
15.
Analysis of 13 cell types reveals evidence for the expression of numerous novel primate- and tissue-specific microRNAs.
Proc Natl Acad Sci U S A
; 112(10): E1106-15, 2015 Mar 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-25713380
16.
Establishment of an orthotopic patient-derived xenograft mouse model using uveal melanoma hepatic metastasis.
J Transl Med
; 15(1): 145, 2017 06 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-28645290
17.
Nanostructured luminescently labeled nucleic acids.
Luminescence
; 32(2): 132-141, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-27417153
18.
Human platelet microRNA-mRNA networks associated with age and gender revealed by integrated plateletomics.
Blood
; 123(16): e37-45, 2014 Apr 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-24523238
19.
Detection and Characterization of Circulating Tumor Associated Cells in Metastatic Breast Cancer.
Int J Mol Sci
; 17(10)2016 Sep 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-27706044
20.
Clinical exome performance for reporting secondary genetic findings.
Clin Chem
; 61(1): 213-20, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25414276